Canonical Allele Identifier: CA4321436
Gene: PCLO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83155140A>G , CM000669.2:g.83155140A>G GRCh38
NC_000007.13:g.82784456A>G , CM000669.1:g.82784456A>G GRCh37
NC_000007.12:g.82622392A>G NCBI36
NG_047145.1:g.12742T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333891.14:c.1501T>C MANE Select ENSP00000334319.8:p.Ser501Pro
ENST00000333891.13:c.1501T>C ENSP00000334319.8:p.Ser501Pro
ENST00000423517.6:c.1501T>C ENSP00000388393.2:p.Ser501Pro
NM_014510.2:c.1501T>C NP_055325.2:p.Ser501Pro
NM_033026.5:c.1501T>C NP_149015.2:p.Ser501Pro
XM_017012006.2:c.1501T>C XP_016867495.1:p.Ser501Pro
XM_017012007.1:c.1501T>C XP_016867496.1:p.Ser501Pro
XR_001744643.2:n.3070T>C
NM_033026.6:c.1501T>C MANE Select NP_149015.2:p.Ser501Pro
NM_014510.3:c.1501T>C NP_055325.2:p.Ser501Pro